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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432207Erstellt: 25. Oktober 2026

N-Ethyl-N-benzylaniline → N-benzyl-N-(4-bromophenyl)-N-ethylamine

https://huagongshe.com/reaction/432207

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Ethyl-N-benzylanilineHCID 7098—
Edukt2,4,4,6-Tetrabromocyclohexa-2,5-dienoneHCID 88433—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-benzyl-N-(4-bromophenyl)-N-ethylamineHCID 2234735076,6%

Reaktionsschritte

N-benzyl-N-phenyl-N-ethylamine (2.25 g, 0.0107 mol) was dissolved in anhydrous dichloromethane (80 mL) and 2,4,4,6-tetrabromocyclohexadiene-1-one (4.36 g, 0.0107 mol) was added in 6 equal portions over a 20 min. period. Stirring was continued at ambient temperature for 20 hours; the organic phase was successively washed with 0.5N solution of sodium hydroxide in water (50 mL), 1N solution of sodium hydroxide in water (50 mL), water (70 mL) and brine (75 mL). The organic phase was dried with magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (1:99) as mobile phase to yield N-benzyl-N-(4-bromophenyl)-N-ethylamine (2.38 g, 0.0082 mol) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660744B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-accf4bcf582142b2b40bfe74ca528ad4
Quellennotizuspto-grants-2003_12